Structure-activity relationships in carboxamide derivatives based on the targeted delivery of radionuclides and boron atoms by means of peripheral benzodiazepine receptor ligands

被引:38
作者
Cappelli, A
Mohr, GL
Gallelli, A
Giuliani, G
Anzini, AM
Vomero, S
Fresta, M
Porcu, P
Maciocco, E
Concas, A
Biggio, G
Donati, A
机构
[1] Univ Siena, Dipartimento Farmaco Chim Tecnol, I-53100 Siena, Italy
[2] Univ Magna Graecia, Dipartimento Sci Farmacobiol, I-88021 Catanzaro, Italy
[3] Univ Cagliari, Dipartimento Biol Sperimentale B Loddo, I-09042 Monserrato, Cagliari, Italy
[4] Univ Siena, Dipartimento Sci & Technol Chim & Biosistemi, I-53100 Siena, Italy
关键词
D O I
10.1021/jm034068b
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The structure-activity relationship studies on 2-quinolinecarboxamide peripheral benzodiazepine receptor (PBR) ligands have been refined with the aim of using these ligands as carriers of radionuclides and boron atoms. Some new ligands show enhanced affinity and steroidogenic activity with respect to reference compound 1 and are interesting candidates for radiolabeling and PET studies. Moreover, carborane derivative 3q, representing the first example of PBR ligand bearing a carborane cage, can be useful to explore an alternative mechanism in BNCT.
引用
收藏
页码:3568 / 3571
页数:4
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